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慢性腰痛服用阿片类药物患者中潜在 CYP450 药代动力学药物相互作用暴露的流行率。

Prevalence of exposure to potential CYP450 pharmacokinetic drug-drug interactions among patients with chronic low back pain taking opioids.

机构信息

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Pain Pract. 2011 May-Jun;11(3):230-9. doi: 10.1111/j.1533-2500.2010.00413.x. Epub 2010 Aug 27.

DOI:10.1111/j.1533-2500.2010.00413.x
PMID:20807350
Abstract

Drug-drug interactions (DDIs) have been defined as two or more drugs interacting in such a way that the effectiveness and/or toxicity of one or all drugs are changed. Patients taking more than one drug metabolized through the cytochrome P450 (CYP450) enzyme system, including some, but not all, opioids experience a drug-drug exposure (DDE), which may result in a potentially dangerous DDI. Using a retrospective analysis of a large commercial claims database and a Medicare database, we evaluated DDEs that have the potential to cause DDIs among chronic low back pain (cLBP) patients on long-term opioid analgesia, which metabolizes through the CYP450 enzyme system, concomitant with other CYP450-metabolized drug(s). The overall prevalence of DDEs among cLBP patients was 27%. Women had a higher prevalence of DDEs (30.6% vs. 22% for men). Patients aged 45 to 55 and 56 to 64 years had the highest prevalence of DDEs (30.4% and 29.8%, respectively), followed by patients 34 to 45 years (27.9%). For patients>65 years, the prevalence of DDEs was 23.1%. In general, the prevalence of DDEs was fairly consistent across age ranges in this population. This study suggests that DDEs are common in the cLBP population. When selecting an opioid to treat cLBP, physicians should consider the potential for exposure of these patients to drugs that might unfavorably interact and, for that reason, the use of opioids that do not rely on the CYP450 system as their primary means of metabolism might be worthy of consideration.

摘要

药物-药物相互作用(DDI)被定义为两种或多种药物以某种方式相互作用,以致一种或所有药物的疗效和/或毒性发生改变。接受一种或多种通过细胞色素 P450(CYP450)酶系统代谢的药物治疗的患者,包括但不限于一些阿片类药物,会经历药物-药物暴露(DDE),这可能导致潜在危险的 DDI。本研究通过对大型商业索赔数据库和医疗保险数据库进行回顾性分析,评估了长期接受阿片类药物镇痛治疗的慢性下背痛(cLBP)患者中,可能导致 CYP450 代谢药物相互作用的 DDE。cLBP 患者中 DDE 的总体发生率为 27%。女性 DDE 的发生率更高(30.6% vs. 男性 22%)。45-55 岁和 56-64 岁的患者 DDE 发生率最高(分别为 30.4%和 29.8%),其次是 34-45 岁的患者(27.9%)。对于>65 岁的患者,DDE 的发生率为 23.1%。一般来说,在该人群中,DDE 的发生率在各年龄段之间相当一致。本研究表明,DDE 在 cLBP 人群中很常见。在选择阿片类药物治疗 cLBP 时,医生应考虑到这些患者接触可能不利相互作用的药物的可能性,因此,使用不依赖 CYP450 系统作为主要代谢途径的阿片类药物可能值得考虑。

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